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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078996Generated: November 2, 2026

Potassium Carbonate → 9-cyano-N-(2,4-dichlorophenyl)-N-methyl-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carboxamide

https://huagongshe.com/reaction/2078996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantOxalyl chlorideHCID 65578—
Reactant2,4-Dichloro-N-methylanilineHCID 2800935—
Reactant9-Cyano-4,5-dihydro-6-oxa-1-thia-benzo[e]azulene-2-carboxylic acidHCID 56834156—
CatalystDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product9-cyano-N-(2,4-dichlorophenyl)-N-methyl-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carboxamideHCID 57900252—

Reaction Steps

To a solution of 9-cyano-4,5-dihydro-6-oxa-1-thia-benzo[e]azulene-2-carboxylic acid (300 mg) in dichloromethane (10 mL) was added DMF (1 drop) and oxalyl chloride (0.165 mL) and the reaction stirred at room temperature for 30 min. The solvent was then reduced in vacuo and the residue redissolved in acetonitrile (10 mL). To this solution was added 2,4-dichloro-N-methylaniline (0.16 mL) and potassium carbonate (308 mg) and the reaction stirred at room temperature for 16 h. The mixture was partitioned between water (40 mL) and ethyl acetate (30 mL). The organic layer was dried (Na2SO4), reduced in vacuo and purified on silica to give 336. (CDCl3): 3.11 (2H, t), 3.39 (3H, s), 4.32 (2H, t), 6.91 (1H, s), 7.07 (1H, d), 7.32 (1H, d), 7.37-7.44 (2H, m), 7.58 (1H, s), 7.79 (1H, s). MH+ 429:431:433 (3:2:1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928248B2
Source datasetuspto-grants-2011_04
ORD IDord-d786408e6ed2429aa8a33d0619c8170a
Source noteuspto-grants-2011_04